RS199469464 SRCAP

Health Risk Chr 16:30737370
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Floating-Harbor syndrome
Inborn genetic diseases
See cases
Neurodevelopmental delay
Developmental delay
hypotonia
musculoskeletal defects
and behavioral abnormalities
SRCAP-related disorder
Monogenic short statue
Floating-Harbor syndrome
Inborn genetic diseases
See cases
Neurodevelopmental delay
Developmental delay
Other Variants in SRCAP
rs199469465 rs199469466 rs587776938 rs587777656 rs587784443 rs587784444 rs200175704 rs144476508 rs150413453 rs138152469
Ask Dr. Hemsworth about this variant